Tryptophol

• Catalog No.: Bio-0306
• CAS Number: 526-55-6
• M. F.: C10H11NO
• M. W.: 161.20044

SYNONYMS

• IUPAC name: 2-(1H-indol-3-yl)ethan-1-ol
• IUPAC Traditional name: 2-(1H-indol-3-yl)ethan-1-ol
• Synonyms: 2-(3-Indolyl)ethanol; 3-(2-Hydroxyethyl)indole

DATABASE IDS

• CAS Number: 526-55-6

PROPERTIES

• Application(s): Active against gram-positive bacteria and Candida albicans
• Biological Source: From Tryptophan fermentations, plant seedlings and Candida spp., Aspergillus niger, Agrobacterium tumefaciens, Ceratocystis spp. and Rhizobium spp.
• Mechanism of Action: Inhibitor of amyloid formation
• Mechanism of Action: Inhibitor of androgen receptor expression

REFERENCES

• Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 3, 130A, (nmr)
• Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 659B, (ir)
• Aldrich Library of FT-IR Spectra: Vapor Phase, 1989, 3, 1502A, (ir)
• Ehrlich, F., Ber., 1912, 45, 884
• Jackson, R.W., J. Biol. Chem., 1930, 88, 659
• Oddo, B. et al., Gazz. Chim. Ital., 1937, 69, 10
• Snyder, H.R. et al., J.A.C.S., 1948, 70, 3770
• Fish, M.S. et al., J.A.C.S., 1959, 78, 3668
• Nogrady, T. et al., Can. J. Chem., 1964, 42, 485
• Narayanan, T.K. et al., Antimicrob. Agents Chemother., 1976, 9, 375, (isol, props)
• Ayer, W.A. et al., Can. J. Chem., 1986, 64, 904, (isol)
• Bhlendorf, B. et al., Annalen, 1996, 49, (isol, ir, pmr, cmr, ms)
• Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, ICS000